A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048430



Internal ID19137649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85750412..85777751hg38UCSC Ensembl
Innerchr15:86293643..86320982hg19UCSC Ensembl
Innerchr15:84094647..84121986hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3827340
hg1927340
hg1827340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2649n100
Supporting Variantsnssv3555084
Samples
Known GenesKLHL25, MIR1276
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048430
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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